Canonical Allele Identifier: CA348180509
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990666G>T , CM000664.2:g.120990666G>T GRCh38
NC_000002.11:g.121748242G>T , CM000664.1:g.121748242G>T GRCh37
NC_000002.10:g.121464712G>T NCBI36
NG_009030.1:g.198376G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4701G>T MANE Select ENSP00000354586.5:p.Met1567Ile
ENST00000452319.6:c.4752G>T ENSP00000390436.1:p.Met1584Ile
ENST00000341310.10:c.*3800G>T ENSP00000344473.6:n.*3800G>T
ENST00000361492.8:c.4752G>T ENSP00000354586.4:p.Met1584Ile
ENST00000438299.5:c.*2620G>T ENSP00000400593.1:n.*2620G>T
ENST00000445186.5:c.*3851G>T ENSP00000397488.1:n.*3851G>T
ENST00000452319.5:c.4752G>T ENSP00000390436.1:p.Met1584Ile
ENST00000452692.5:c.*2569G>T ENSP00000403715.1:n.*2569G>T
NM_005270.4:c.4752G>T NP_005261.2:p.Met1584Ile
XM_006712422.1:c.4701G>T XP_006712485.1:p.Met1567Ile
XM_011510969.1:c.4734G>T XP_011509271.1:p.Met1578Ile
XM_011510970.1:c.4611G>T XP_011509272.1:p.Met1537Ile
XM_011510971.1:c.4557G>T XP_011509273.1:p.Met1519Ile
XM_011510972.1:c.4557G>T XP_011509274.1:p.Met1519Ile
XM_011510973.1:c.4377G>T XP_011509275.1:p.Met1459Ile
XM_011510974.1:c.4326G>T XP_011509276.1:p.Met1442Ile
XM_006712422.3:c.4701G>T XP_006712485.1:p.Met1567Ile
XM_011510969.2:c.5004G>T XP_011509271.2:p.Met1668Ile
XM_011510970.2:c.4611G>T XP_011509272.1:p.Met1537Ile
XM_011510971.2:c.4557G>T XP_011509273.1:p.Met1519Ile
XM_011510972.2:c.4653G>T XP_011509274.2:p.Met1551Ile
XM_011510973.2:c.4377G>T XP_011509275.1:p.Met1459Ile
XM_011510974.2:c.4326G>T XP_011509276.1:p.Met1442Ile
XM_017003818.1:c.4953G>T XP_016859307.1:p.Met1651Ile
XM_024452794.1:c.4752G>T XP_024308562.1:p.Met1584Ile
XM_024452795.1:c.4752G>T XP_024308563.1:p.Met1584Ile
NM_001371271.1:c.4752G>T NP_001358200.1:p.Met1584Ile
NM_001374353.1:c.4701G>T MANE Select NP_001361282.1:p.Met1567Ile
NM_001374354.1:c.4326G>T NP_001361283.1:p.Met1442Ile
NM_005270.5:c.4752G>T NP_005261.2:p.Met1584Ile